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FDA 510(k)

SEALANT, NEW FILLED

K-Number: K760405 · 1976-08-23

ApplicantL.D. Caulk Co.
Decision Date1976-08-23
Product CodeEBC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SEALANT, NEW FILLED is the device name listed in this FDA 510(k) record. The listed applicant is L.D. Caulk Co.. It received FDA 510(k) clearance on 1976-08-23 under 510(k) number K760405. The device is classified under product code EBC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEALANT, NEW FILLED?

SEALANT, NEW FILLED is a medical device that received FDA 510(k) clearance on 1976-08-23. The listed applicant is L.D. Caulk Co.. The 510(k) number is K760405.

When did SEALANT, NEW FILLED receive FDA 510(k) clearance?

SEALANT, NEW FILLED received FDA 510(k) clearance on 1976-08-23, under 510(k) number K760405.

Who is the listed applicant for SEALANT, NEW FILLED?

The FDA 510(k) record lists L.D. Caulk Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SEALANT, NEW FILLED?

The FDA product code for SEALANT, NEW FILLED is EBC.

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Other records listing L.D. Caulk Co. as applicant

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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